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Description

Basic Functions to Investigate Metabolomics Data Matrices.

A set of functions to investigate raw data from (metabol)omics experiments intended to be used on a raw data matrix, i.e. following peak picking and signal deconvolution. Functions can be used to normalize data, detect biomarkers and perform sample classification. A detailed description of best practice usage may be found in the publication <doi:10.1007/978-1-4939-7819-9_20>.

MetabolomicsBasics

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The goal of MetabolomicsBasics is to provide a set of functions to investigate raw data (a matrix of intensity values) from (metabol)omics experiments, i.e.  following peak picking and signal deconvolution. Functions can be used to i.e.:

  • normalize data
  • detect biomarkers
  • perform sample classification

A detailed description of best practice usage may be found in the publication https://link.springer.com/protocol/10.1007/978-1-4939-7819-9_20.

Installation

You can install the development version of MetabolomicsBasics from GitHub with:

# install.packages("devtools")
devtools::install_github("janlisec/MetabolomicsBasics")

Examples

A typical use case would be to compute a Principal Component Analysis:

raw <- MetabolomicsBasics::raw
sam <- MetabolomicsBasics::sam
MetabolomicsBasics::RestrictedPCA(dat = raw, sam = sam, group.col = "Group", legend.x = "bottomleft", medsd = TRUE, fmod = "Group")

More elaborate plots, like the polar coordinate visualization of heterosis pattern are possible:

x <- t(raw)
colnames(x) <- sam$GT
MetabolomicsBasics::PolarCoordHeterPlot(x=x, gt=c("B73","B73xMo17","Mo17"), plot_lab="graph", col=1:10, thr=0.5, rev_log=exp(1))
#> Parameter 'col' should be a color vector of length nrow(x)
Metadata

Version

1.4.5

License

Unknown

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